OBO ID: DOID:0111795 |
Term Name: | congenital nystagmus 6 | Search Ontology: | |
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Definition: | A congenital nystagmus that has_material_basis_in hemizygous of homoxygous mutation in the GPR143 gene on chromosome Xp22.2. https://www.ncbi.nlm.nih.gov/pubmed/17516023 | ||
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Ontology: | Human Disease ( DOID:0111795 ) |
OTHER congenital nystagmus 6 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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